作者：
Conroy,J. [1]
;
McGettigan,P.A. [2]
;
McCreary,D. [3]
;
Shah,N. [4]
;
Collins,K. [5]
;
Parry-Fielder,B. [6]
;
Moran,M. [7]
;
Hanrahan,D. [8]
;
Deonna,T.W. [9]
;
Korff,C.M. [10]
;
Webb,D. ;
Ennis,S. ;
Lynch,S.A. ;
King,M.D.
作者单位：
Department of Neurology, Children's University Hospital, Dubline, Ireland, Royal Children's
[1]
Department of Neurology, Our Lady's Children's Hospital Crumlin, Dubline, Ireland
[2]
Royal Children's Hospital, Melbourne VIC, Australia
[3]
Department of Neurology, Children's University Hospital, Dubline, Ireland
[4]
School of Medicine and Medical Science, University College Dublin, Dubline, Ireland
[5]
Royal Belfast Hospital for Sick Children, Belfast, United Kingdom
[6]
University Hospitals, Geneva, Switzerland
[7]
Academic Centre on Rare Diseases, School of Medicine and Medical Science, University College Dublin
[8]
Department of Genetics, Children's University Hospital, Dubline, Ireland, Academic Centre on Rare
[9]
University Hospital of Lausanne, Lausanne, Switzerland
[10]
发布时间
2018-09-20
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